Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca4 |
T |
C |
3: 121,967,637 (GRCm39) |
L2229P |
possibly damaging |
Het |
Acaca |
T |
A |
11: 84,151,460 (GRCm39) |
M786K |
probably damaging |
Het |
Adap1 |
T |
G |
5: 139,278,928 (GRCm39) |
E117D |
possibly damaging |
Het |
Ap5z1 |
T |
C |
5: 142,463,053 (GRCm39) |
S746P |
probably benign |
Het |
Appl2 |
A |
G |
10: 83,453,292 (GRCm39) |
I208T |
possibly damaging |
Het |
Astn1 |
A |
G |
1: 158,332,956 (GRCm39) |
E346G |
possibly damaging |
Het |
Astn1 |
G |
A |
1: 158,495,208 (GRCm39) |
|
probably null |
Het |
Atp23 |
T |
A |
10: 126,704,594 (GRCm39) |
I180L |
unknown |
Het |
Bean1 |
CT |
C |
8: 104,908,664 (GRCm39) |
|
probably null |
Het |
Cdh23 |
A |
T |
10: 60,220,724 (GRCm39) |
I1340N |
probably benign |
Het |
Cdh8 |
G |
A |
8: 99,825,517 (GRCm39) |
Q493* |
probably null |
Het |
Ces1g |
T |
C |
8: 94,046,455 (GRCm39) |
I357V |
probably benign |
Het |
Ddx46 |
A |
G |
13: 55,798,291 (GRCm39) |
D226G |
probably damaging |
Het |
Eea1 |
C |
T |
10: 95,830,767 (GRCm39) |
Q143* |
probably null |
Het |
Erlin2 |
G |
T |
8: 27,521,800 (GRCm39) |
|
probably null |
Het |
Fat3 |
T |
A |
9: 15,849,615 (GRCm39) |
D3929V |
probably damaging |
Het |
Flt3 |
T |
C |
5: 147,271,247 (GRCm39) |
D898G |
probably damaging |
Het |
Gm16519 |
A |
G |
17: 71,236,351 (GRCm39) |
N100S |
probably benign |
Het |
Gnl1 |
A |
G |
17: 36,299,428 (GRCm39) |
H533R |
probably damaging |
Het |
Gphn |
A |
G |
12: 78,551,454 (GRCm39) |
T301A |
possibly damaging |
Het |
Herc2 |
C |
T |
7: 55,869,527 (GRCm39) |
R4295* |
probably null |
Het |
Insm2 |
T |
C |
12: 55,646,303 (GRCm39) |
S16P |
possibly damaging |
Het |
Jak2 |
C |
T |
19: 29,276,037 (GRCm39) |
T778I |
probably benign |
Het |
Lrriq3 |
A |
G |
3: 154,806,734 (GRCm39) |
T128A |
probably damaging |
Het |
Lst1 |
A |
G |
17: 35,405,920 (GRCm39) |
|
probably null |
Het |
Magi1 |
G |
T |
6: 93,685,091 (GRCm39) |
Y762* |
probably null |
Het |
Man2b1 |
T |
A |
8: 85,817,594 (GRCm39) |
C358* |
probably null |
Het |
Mga |
T |
C |
2: 119,766,032 (GRCm39) |
V1432A |
probably damaging |
Het |
Mmp1a |
TG |
TGG |
9: 7,465,083 (GRCm38) |
|
probably null |
Het |
Morc2a |
C |
T |
11: 3,633,566 (GRCm39) |
Q587* |
probably null |
Het |
Mrc2 |
T |
C |
11: 105,183,623 (GRCm39) |
I4T |
probably benign |
Het |
Muc16 |
C |
A |
9: 18,549,431 (GRCm39) |
V5621F |
probably benign |
Het |
Myl10 |
G |
C |
5: 136,726,825 (GRCm39) |
V70L |
probably benign |
Het |
Myo3b |
A |
G |
2: 70,047,513 (GRCm39) |
R340G |
probably benign |
Het |
Nipal3 |
T |
C |
4: 135,218,248 (GRCm39) |
Y34C |
probably damaging |
Het |
Nktr |
T |
A |
9: 121,578,345 (GRCm39) |
D804E |
unknown |
Het |
Nlrp4b |
A |
G |
7: 10,448,816 (GRCm39) |
M340V |
probably benign |
Het |
Or1e26 |
T |
A |
11: 73,480,094 (GRCm39) |
T157S |
probably benign |
Het |
Or2ag2b |
G |
A |
7: 106,417,581 (GRCm39) |
C97Y |
probably damaging |
Het |
Or56a41 |
A |
T |
7: 104,741,978 (GRCm39) |
M16K |
probably benign |
Het |
Or5al5 |
A |
G |
2: 85,961,608 (GRCm39) |
V133A |
probably benign |
Het |
Pard3 |
T |
A |
8: 128,337,063 (GRCm39) |
N1271K |
probably damaging |
Het |
Pcdhb11 |
A |
T |
18: 37,554,672 (GRCm39) |
M1L |
possibly damaging |
Het |
Pclo |
T |
C |
5: 14,732,118 (GRCm39) |
V3540A |
unknown |
Het |
Pemt |
A |
G |
11: 59,867,670 (GRCm39) |
F154S |
probably damaging |
Het |
Ptpn18 |
G |
A |
1: 34,512,445 (GRCm39) |
D417N |
possibly damaging |
Het |
Rnpc3 |
G |
T |
3: 113,407,481 (GRCm39) |
T376K |
probably benign |
Het |
Rpe65 |
A |
G |
3: 159,310,246 (GRCm39) |
Y143C |
probably damaging |
Het |
Sbk2 |
T |
C |
7: 4,966,148 (GRCm39) |
E12G |
probably benign |
Het |
Slc2a5 |
T |
C |
4: 150,213,526 (GRCm39) |
I106T |
possibly damaging |
Het |
Snx13 |
A |
G |
12: 35,135,981 (GRCm39) |
D92G |
probably damaging |
Het |
Sorl1 |
C |
T |
9: 41,891,984 (GRCm39) |
V1889I |
probably benign |
Het |
Spag17 |
A |
T |
3: 99,846,563 (GRCm39) |
N29I |
possibly damaging |
Het |
Speg |
T |
C |
1: 75,378,108 (GRCm39) |
V878A |
probably damaging |
Het |
Timp4 |
A |
G |
6: 115,227,421 (GRCm39) |
S53P |
probably damaging |
Het |
Tssk1 |
G |
T |
16: 17,712,948 (GRCm39) |
E244D |
probably benign |
Het |
Usp29 |
A |
C |
7: 6,964,219 (GRCm39) |
T21P |
possibly damaging |
Het |
Vmn2r85 |
A |
T |
10: 130,258,735 (GRCm39) |
V440E |
probably benign |
Het |
Wdr59 |
T |
C |
8: 112,217,001 (GRCm39) |
D270G |
|
Het |
Zbbx |
G |
A |
3: 74,992,826 (GRCm39) |
P223S |
probably damaging |
Het |
Zfp936 |
T |
A |
7: 42,839,239 (GRCm39) |
C235* |
probably null |
Het |
Zranb3 |
A |
T |
1: 127,960,584 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Acta2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01660:Acta2
|
APN |
19 |
34,229,191 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01802:Acta2
|
APN |
19 |
34,220,836 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL01945:Acta2
|
APN |
19 |
34,229,254 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02136:Acta2
|
APN |
19 |
34,229,230 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03114:Acta2
|
APN |
19 |
34,222,310 (GRCm39) |
critical splice donor site |
probably null |
|
R0648:Acta2
|
UTSW |
19 |
34,225,934 (GRCm39) |
missense |
probably benign |
|
R1393:Acta2
|
UTSW |
19 |
34,219,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R1597:Acta2
|
UTSW |
19 |
34,229,983 (GRCm39) |
splice site |
probably benign |
|
R2045:Acta2
|
UTSW |
19 |
34,220,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R2338:Acta2
|
UTSW |
19 |
34,225,941 (GRCm39) |
splice site |
probably benign |
|
R3113:Acta2
|
UTSW |
19 |
34,220,752 (GRCm39) |
missense |
probably benign |
|
R3940:Acta2
|
UTSW |
19 |
34,220,880 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3955:Acta2
|
UTSW |
19 |
34,229,126 (GRCm39) |
splice site |
probably benign |
|
R4765:Acta2
|
UTSW |
19 |
34,223,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R4826:Acta2
|
UTSW |
19 |
34,229,223 (GRCm39) |
nonsense |
probably null |
|
R6453:Acta2
|
UTSW |
19 |
34,224,057 (GRCm39) |
missense |
probably damaging |
1.00 |
R6754:Acta2
|
UTSW |
19 |
34,222,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R6941:Acta2
|
UTSW |
19 |
34,229,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R7311:Acta2
|
UTSW |
19 |
34,219,186 (GRCm39) |
missense |
probably damaging |
1.00 |
R7461:Acta2
|
UTSW |
19 |
34,229,931 (GRCm39) |
missense |
probably benign |
0.00 |
R7463:Acta2
|
UTSW |
19 |
34,229,931 (GRCm39) |
missense |
probably benign |
0.00 |
R7464:Acta2
|
UTSW |
19 |
34,229,931 (GRCm39) |
missense |
probably benign |
0.00 |
R7536:Acta2
|
UTSW |
19 |
34,229,931 (GRCm39) |
missense |
probably benign |
0.00 |
R7605:Acta2
|
UTSW |
19 |
34,229,931 (GRCm39) |
missense |
probably benign |
0.00 |
R7609:Acta2
|
UTSW |
19 |
34,229,931 (GRCm39) |
missense |
probably benign |
0.00 |
R7610:Acta2
|
UTSW |
19 |
34,229,931 (GRCm39) |
missense |
probably benign |
0.00 |
R7611:Acta2
|
UTSW |
19 |
34,229,931 (GRCm39) |
missense |
probably benign |
0.00 |
R7613:Acta2
|
UTSW |
19 |
34,229,931 (GRCm39) |
missense |
probably benign |
0.00 |
R7626:Acta2
|
UTSW |
19 |
34,229,931 (GRCm39) |
missense |
probably benign |
0.00 |
R7627:Acta2
|
UTSW |
19 |
34,229,931 (GRCm39) |
missense |
probably benign |
0.00 |
R7803:Acta2
|
UTSW |
19 |
34,220,818 (GRCm39) |
missense |
probably benign |
|
R7872:Acta2
|
UTSW |
19 |
34,220,839 (GRCm39) |
missense |
probably damaging |
0.99 |
R8801:Acta2
|
UTSW |
19 |
34,229,207 (GRCm39) |
missense |
probably damaging |
0.99 |
R9059:Acta2
|
UTSW |
19 |
34,219,155 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9191:Acta2
|
UTSW |
19 |
34,222,480 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9487:Acta2
|
UTSW |
19 |
34,225,865 (GRCm39) |
missense |
probably damaging |
0.99 |
R9675:Acta2
|
UTSW |
19 |
34,223,612 (GRCm39) |
missense |
|
|
R9776:Acta2
|
UTSW |
19 |
34,223,481 (GRCm39) |
missense |
probably benign |
0.01 |
|